Methotrexate composition

ABSTRACT

A Methotrexate composition for oral administration is provided comprising a pharmaceutically acceptable salt of Methotrexate and an aqueous carrier agent. The Methotrexate salt is substantially or completely soluble in the aqueous carrier agent, forming an aqueous solution. There is also provided a method of manufacturing a Methotrexate composition for oral administration, comprising mixing a pharmaceutically acceptable salt of Methotrexate with an aqueous carrier agent until the Methotrexate salt is substantially or completely soluble in the carrier agent to form an aqueous solution.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation application of U.S. Ser. No. 13/733,031 filed Jan. 2, 2013 which claims priority to British Patent Application No. 1200192.1 filed 6 Jan. 2012, each of which is incorporated herein by reference.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Non-applicable

THE NAMES OF THE PARTIES TO A JOINT RESEARCH AGREEMENT

Non-applicable

REFERENCE TO A “SEQUENCE LISTING”

Non-applicable

BACKGROUND OF THE INVENTION

This invention relates to a Methotrexate composition, a method of use thereof and a method of manufacture.

Methotrexate has the systemic name of (2S)-2-[(4-{[2,4-diaminopteridin-6-yl)methyl](methyl)amino}benzoyl)amino] pentanedioic acid or C₂₀H₂₂N₈O₅. It is used as a folic acid antagonist, in the treatment of neoplastic disease, such as trophoblastic neoplasms and leukaemia and in the control of severe recalcitrant psoriasis which is not responsive to other forms of therapy. It is also used to treat a wide range of tumours, such as acute leukaemias, Non-Hodgkin's lymphoma, soft tissue and bone sarcomas, solid tumours like breast, lung, head, neck, bladder, cervical, ovarian and testicular cancer, as an immunosuppressant and as an anti-metabolite.

Use of Methotrexate containing compositions for oral administration in tablet form is known. However, a solid tablet form may be unsuitable for patients who have difficulty swallowing, such as children, elderly patients, stroke patients and/or the like. In order to overcome this problem, it would be beneficial to provide a Methotrexate containing composition as an oral solution which is palatable, as well as physically and chemically stable. However, Methotrexate has been found to precipitate out of solution over time.

BRIEF SUMMARY OF THE INVENTION

It is therefore an aim of the present invention to provide an optimised Methotrexate composition suitable for oral administration which overcomes the abovementioned problems.

It is a further aim of the present invention to provide a method of manufacturing an improved Methotrexate composition suitable for oral administration.

It is a yet further aim of the present invention to provide a method of use of an improved Methotrexate composition for oral administration.

According to a first aspect of the present invention there is provided a Methotrexate composition suitable for oral administration, said composition containing a pharmaceutically acceptable salt of Methotrexate and an aqueous carrier agent in which the Methotrexate salt is substantially or completely soluble to form an aqueous solution.

The Methotrexate solution as described herein is stable in that it remains substantially or wholly dissolved in the aqueous agent for a prolonged or predetermined period of time. The term “solution” is in contrast to a Methotrexate containing “suspension” wherein the Methotrexate salt is un-dissolved and homogenously dispersed in a suspension medium.

Any pharmaceutically acceptable soluble salt of Methotrexate can be used. Preferably the pharmaceutically acceptable soluble salt of Methotrexate used is Methotrexate disodium. This salt is preferably in a powder form prior to addition to the aqueous carrier agent.

Preferably the pH of the composition is within the pH range of 6-7. It has been found by the Applicants that at pH values below 6.0 the Methotrexate is seen to precipitate out of solution over time and the lower the pH the greater the amount of precipitate seen. At pH values above 7.0 there is an increase in degradation that will limit the shelf life of the composition.

Further preferably the pH of the composition is within the pH range of 6.1-6.5. Yet further preferably the pH of the composition is at pH 6.25+/−0.15.

Preferably the aqueous carrier agent is or includes water, purified water and/or the like.

Preferably the composition includes one or more buffer agents or pH modifying agents to adjust the pH to the preferred range. The combination of the pH range used and the buffer strength of the one or more buffer agents typically prevent precipitation of the Methotrexate and maintain the composition as a substantially clear solution.

The one or more buffer agents can include any or any combination of Citric Acid, Sodium Citrate, Sodium Dihydrogen Phosphate, Disodium Hydrogen Phosphate, Trometamol (Tris), Hydrochloric Acid, Ascorbic Acid, Sodium Ascorbate, any of the abovementioned sodium salts replaced with potassium salts and/or the like.

Preferably two or more buffer agents are provided to form a buffer system, such as a Citric Acid-Sodium Citrate Buffer, Sodium Dihydrogen Phosphate-Disodium Hydrogen Phosphate Buffer, Trometamol (Tris)-Hydrochloric Acid Buffer, Trometamol (Tris)-Citric Acid Buffer, Ascorbic Acid-Sodium Ascorbate Buffer, any of the abovementioned sodium salts replaced with potassium salts and/or the like.

In a preferred embodiment the two or more buffer agents include citric acid monohydrate and disodium hydrogen phosphate.

Preferably the resulting buffer strength used is in the range of 2 millimolar to 200 millimolar. Further preferably the resulting buffer strength used is in the range of 2-20 millimolar to maximise the stability of the Methotrexate and shelf life of the oral solution product.

Preferably the composition includes one or more preserving agents to increase the shelf life of the composition. The one or more preserving agents could include any or any combination of Sodium Methyl Hydroxybenzoate, Sodium Ethyl Hydroxybenzoate, Sodium Propyl Hydroxybenzoate, Sodium Benzoate, Potassium Sorbate and/or the like.

Preferably the composition includes one or more flavouring compounds and/or sweetening agents to mask the taste of the Methotrexate salt contained therein and/or to make the resulting composition more palatable. The one or more flavouring compounds and/or sweetening agents can include Sucralose, Acesulfame K, any other water soluble sweetener, Raspberry Flavour 545742E and/or the like that is/are compatible with the Methotrexate salt used in the composition.

In one embodiment the Methotrexate composition can be used in the treatment of or for the manufacture of a medicament for the treatment of any or any combination of a folic acid antagonist, an anti-neoplastic agent, an immunosuppressant, an anti-metabolite, neoplastic disease, malignant disease, psoriasis, Crohn's disease, rheumatoid arthritis, polyarthritic forms of active juvenile idiopathic arthritis, juvenile dermatomyositis, vasculitis, uvenlitis, systemic lupus erythematosus, localised scleroderma and sarcoidrosis.

Preferably the pharmaceutically acceptable dosage of the Methotrexate salt used in the composition is 2.5 mg/5 ml, 5 mg/5 ml, 10 mg/5 ml or in the range of 0.05 mg/1 ml to 20 mg/1 ml.

In a preferred embodiment the composition includes a pharmaceutically acceptable salt of Methotrexate, one or more buffering agents, one or more preserving agents, one or more sweetener agents and one or more flavourings.

According to a second aspect of the present invention there is provided a method of manufacturing a Methotrexate composition suitable for oral administration, said method including the step of mixing a pharmaceutically acceptable salt of Methotrexate with an aqueous carrier agent until the Methotrexate salt is substantially or completely dissolved in the carrier agent to form an aqueous solution.

Preferably the method of manufacture takes place at room temperature (i.e. between 18-24° C.) and pressure.

The composition can be mixed together using any suitable mixing means.

Storage temperature of the resulting composition is also typically important in the stability of said composition. Preferably the storage temperature of the resulting composition should be at approx. room temperature or within the temperature range of 18-25° C.

According to a further aspect of the present invention there is provided use of a Methotrexate composition in the manufacture of a medicament for the treatment in a patient as a folic acid antagonist, as an anti-neoplastic agent, an immunosuppressant, an anti-metabolite, neoplastic disease, malignant disease, psoriasis, Crohn's disease, rheumatoid arthritis, polyarthritic forms of active juvenile idiopathic arthritis, juvenile dermatomyositis, vasculitis, uvenlitis, systemic lupus erythematosus, localised scleroderma and/or sarcoidrosis, said composition containing a pharmaceutically acceptable salt of Methotrexate and an aqueous carrier agent in which the Methotrexate salt is substantially or completely soluble to form an aqueous solution

Preferably the patient is a human patient.

Thus, the present invention provides a pharmaceutically effective, safe and simple to administer oral dosage form (i.e. oral solution) of Methotrexate that has an increased shelf life and which will benefit a patient group that has problems in swallowing.

BRIEF DESCRIPTION OF THE DRAWING

FIG. 1 is a graph showing results of analysis of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

Detailed embodiments of the present invention will now be described.

Test 1

The Applicants initially undertook a study to calculate the pH at which a Methotrexate composition containing 10 mg/5 ml Methotrexate Disodium remained stable (i.e. showed little or no pH drift over time) and the buffering conditions that provided this stability. The samples in test 1 included Batch A which had the pH adjusted to pH 6 and included buffering agents; Batch B which had been adjusted to pH 6 but contained no buffering agents; and Batch C which had the pH adjusted to 7 and included buffering agents.

More particularly, Batch A included 250 ml of purified water, 5.72 g of Disodium Hydrogen Phosphate Dihydrate, 1.88 g of Citric Acid Monohydrate, 1.096 g* of Methotrexate Disodium and the formulation was made up to 500 ml in purified water. (*Methotrexate Disodium amount includes a QS calculation to account for the sodium salt and raw material water content to produce 10 mg/5 ml of Methotrexate base in the product). The pH was adjusted to pH 6.0 using 10% Citric Acid solution.

Batch B included 250 ml of purified water, 1.096 g* of Methotrexate Disodium and the formulation was made up to 500 ml in purified water. (*Methotrexate Disodium amount includes a QS calculation to account for the sodium salt and raw material water content to produce 10 mg/5 ml of Methotrexate base in the product). The pH was adjusted to pH 6.0 using 10% Citric Acid solution.

Batch C included 250 ml of purified water, 7.76 g of Disodium Hydrogen Phosphate Dihydrate, 0.68 g of Citric Acid Monohydrate, 1.096 g* of Methotrexate Disodium and the formulation was made up to 500 ml in purified water. (*Methotrexate Disodium amount includes a QS calculation to account for the sodium salt and raw material water content to produce 10 mg/5 ml of Methotrexate base in the product). The pH was adjusted to pH 7.0 using 10% Citric Acid solution.

Initially the temperature of the compositions was maintained at 25° C. and the pH was measured at the starting point (t=0), at week 2, week 4 and week 8. The results are shown in Table 1 below.

TABLE 1 Condi- Time - weeks Batch Variables tion 0 2 4 8 A pH 6 Buffered 25° C. pH 5.98 pH 6.09 pH 6.15 pH 6.18 B pH 6 Unbuffered 25° C. pH 6.36 pH 6.51 pH 6.59 pH 7.22 C pH 7.0 Buffered 25° C. pH 6.93 pH 7.02 pH 7.10 pH 7.17 NB: At the time of manufacture the pH of both the pH 6 buffered and pH 6 unbuffered formulations were adjusted to pH 6.00.

Firstly, the results show the instability of the pH of the composition when no buffering agents are used, based on the fact that at T=0 the unbuffered solution of Batch B had already increased to pH 6.36. This suggests that the pH of the Methotrexate solution drifted upwards in the short time between the end of manufacture of the composition and the testing of the samples.

The results from test 1 show that the buffered pH 6.0 and pH 7.0 formulations had minimal pH drift during the study. The unbuffered pH 6.0 formulation showed a marked increase in pH during the study. This test demonstrated that the Methotrexate formulation required a buffer system to control pH drift and to stabilise the resulting composition.

Test 2

The next test was undertaken to determine what effect a buffering system had on the levels of degradants present in a 10 mg/5 ml Methotrexate solution over time. The % of a known degradant (Impurirty E) was measured using an HLPC assay. The same batch samples were made up as for test 1 and the conditions were maintained at 25° C. The % of degradation was measured at the start point (T=0), week 2, week 4 and week 8. The results are shown in Table 2 below.

TABLE 2 Condi- Time - weeks Batch Variables tion 0 2 4 8 A pH 6 Buffered 25° C. 0.00% 0.00% 0.00% 0.13% B pH 6 Unbuffered 25° C. 0.02% 0.10% 0.16% 0.68% C pH 7.0 Buffered 25° C. 0.00% 0.12% 0.19% 1.80%

The results show that even after 8 weeks, the levels of degradation in the Buffered pH 6 formulation remain low throughout the trial with only 0.13% for the 25° C. sample with a corresponding pH of 6.18.

The unbuffered pH 6 formulation showed a much higher level of degradation of 0.68% at a corresponding pH of 7.22.

This data also showed that without a buffer the Methotrexate 10 mg/5 ml formulation showed a tendency for the pH to drift upwards. However, if the pH drifts up to pH 7 or above, the level of the degradation increases rapidly which will limit the shelf-life of the product.

Therefore, it was concluded that it was preferable to use a buffer system in the formulation to obtain a level of stability sufficient for obtaining a prolonged shelf life of the product. In order to choose a suitable buffer system and to calculate the desired buffer strength, a buffer was chosen and comprised an 87 millimolar Citric Acid/Disodium Hydrogen phosphate buffer system. The initial formulation tried was as follows:

Example 1

Ingredient Weight/5 ml Purified Water (A) 3 ml Methotrexate Disodium QS to 10.97 mg Sodium Methyl QS to 4.80 mg Hydroxybenzoate Sodium Ethyl QS to 2.40 mg Hydroxybenzoate Citric Acid Monohydrate 25.0 mg Disodium Hydrogen 57.2 mg Phosphate Dihydrate Sucralose 2.5 mg Raspberry Flavour 545742E 10.0 mg Purified Water (C) To 5 ml QS—Quantum Satis (as much as is required to make up the required volume/weight).

However, on storage a yellow precipitate was seen which was identified as Methotrexate. Therefore further investigation work was carried out to try to identify the causative factors of the precipitate and resolve them.

Batches were prepared at various pHs in the range 5.6-6.0 and were prepared at ½, 1/10^(th) and 1/20^(th) the original buffer strength of example 1 (i.e. the citric acid monohydrate and disodium hydrogen phosphate dihydrate buffer system). The original buffer strength was taken from a citrate-phosphate buffer table (http://microscopy.berkeley.edu/Resources/instruction/buffers.html).

Visual observations showed that both the pH and ionic strength of the buffer affected the rate of precipitation of the Methotrexate (i.e. the point in time at which precipitation is seen) and the amount of Methotrexate precipitate produced.

The graph in FIG. 1 shows the results of the analysis of the filtered supernatant solution for the above Methotrexate formulation at ½ and 1/10^(th) original buffer strength at four different pH values; 5.6, 5.7, 5.8 and 5.9. The analysis is based on the fact that the lower the % of Methotrexate found in the supernatant (i.e. Assay % SA), the lower the amount of Methotrexate remains in solution i.e. fully dissolved. Samples of the supernatant above the precipitate were filtered through a Whatman No. 4 Filter Paper and was assayed using HPLC for the Methotrexate active component.

The results show that by increasing the pH of the formulation towards pH 6.0, this increases the amount of Methotrexate dissolved in the formulation. The results also show that there is less Methotrexate dissolved when a ½ strength buffer system is used compared to the formulation using a 1/10^(th) strength buffer system. This in turn suggests that the Methotrexate composition of the present invention is more physically stable at a lower ionic buffer strength i.e. does not precipitate out of solution.

This analytical work is backed up by stability studies which are shown in Table 3 below. The stability studies were undertaken using the example 1 formulation but using either a citrate-phosphate buffer system at half the strength (i.e. 43 mmol) or 1/10^(th) of the strength (i.e. 8.7 mmol) compared to that of example 1. The formulations were adjusted to 5 different pH values; 5.6, 5.7, 5.8, 5.9 and 6.0. One set of formulations were stored at 5° C. and one set of formulations were stored at 25° C. for each buffer strength and each pH value for the duration of the study. The study took place over a 6 month time period.

TABLE 3 ½ Buffer strength 1/10^(th) Buffer Strength (43 mmol) (8.7 mmol) pH 5° C. 25° C. 5° C. 25° C. 5.6. PPT @ 1 M PPT @ 1 M PPT @ 1 M PPT @ 1 M 5.7 PPT @ 1 M PPT @ 1 M PPT @ 1 M PPT @ 1 M 5.8 PPT @ 1 M PPT @ 1 M PPT @ 1 M PPT @ 1 M 5.9 PPT @ 1 M PPT @ 1 M PPT @ 1 M PPT @ 5 M 6.0 CS @ 6 M CS @ 6 M CS @ 6 M CS @ 6 M PPT—precipitate observed CS—Clear Solution. No precipitate 1 M represents 1 month time period 5 M represents 5 month time period 6 M represents 6 month time period

The results show that visually there was a increase in the amount of Methotrexate in solution as the pH in the formulations increased from 5.6 to 5.9.

Table 4 shows the results of a similar test undertaken using a standard formulation with different ionic strengths of a citrate-phosphate buffer used and all the formulations adjusted to pH 6.0. One set of formulations were kept at 5° C. and one set of formulations were kept at 25° C. for the duration of the study.

Each formulation included 300 g Purified Water, 0.571 g of Sodium Methyl Hydroxybenzoate (equivalent of 0.96 g/L free acid), 0.281 g of Sodium Ethyl Hydroxybenzoate (equivalent to 0.48 g/L free acid), 0.25 g Sucralose, 1 g of Raspberry flavour, 1.293 g Methotrexate Disodium (QS to 2.194 g/L) and made up to 500 ml using Purified Water.

The Citrate-Phosphate control had 5.72 g Disodium Hydrogen Phosphate Dihydrate and 2.50 g of Citric Acid Monohydrate. The Citrate-Phosphate ½ strength buffer had 2.86 g Disodium Hydrogen Phosphate Dihydrate and 1.25 g of Citric Acid Monohydrate. The Citrate-Phosphate 1/10^(th) strength buffer had 0.572 g Disodium Hydrogen Phosphate Dihydrate and 0.250 g of Citric Acid Monohydrate. The Citrate-Phosphate 1/20^(th) strength buffer had 0.286 g Disodium Hydrogen Phosphate Dihydrate and 0.125 g of Citric Acid Monohydrate.

TABLE 4 Buffer Strength Test 5° C. 25° c. Citrate-  87 mmol Appearance PPT @ 2 M PPT @ 6 M Phosphate Degradant NT 0.97% @ 5 M (Control) (Impurity C) Citrate-  43 mmol Appearance PPT @ 3 M CS @ 6 M Phosphate Degradant NT 0.85% @ 5 M (½ strength) (Impurity C) Citrate- 8.7 mmol Appearance CS @ 6 M CS @ 6 M Phosphate Degradant NT 0.76% @ 5 M ( 1/10 strength) (Impurity C) Citrate- 4.3 mmol Appearance CS @ 6 M CS @ 6 M Phosphate Degradant NT 0.70% @ 5 M ( 1/20 strength) (Impurity C) NT—Not Tested PPT—precipitate observed CS—Clear Solution. No precipitate 2 M represents 2 month time period 3 M represents 3 month time period 6 M represents 6 month time period

The results in Table 4 show that the lower the ionic strength of the citrate phosphate buffer, the more stable the formulation is at pH 6.0. No precipitate is observed at a buffer strength of ≤8.7 mmol on storage at 5° C. There is also a decrease in the amount of degradation observed (impurity C) as the buffer strength is decreased.

Table 5 shows a similar test to that undertaken for Table 4 but a separate phosphate and citrate buffers were used.

The formulation of the phosphate buffer used in each sample included 180 g Purified Water, 0.3426 g of Sodium Methyl Hydroxybenzoate *1 (equivalent of 0.96 g/L free acid), 0.1686 g of Sodium Ethyl Hydroxybenzoate *1 (equivalent to 0.48 g/L free acid), 0.15 g Sucralose, 0.6 g of Raspberry flavour, 0.7758 g of Methotrexate Disodium (QS to 2.194 g/L) and made up to 300 ml using Purified Water.

In the 66 mmol phosphate buffer the formulation included 0.357 g of Disodium Hydrogen Phosphate Dihydrate and 2.82 g of Sodium Dihydrogen Phosphate Dihydrate. In the 33 mmol phosphate buffer the formulation included 0.1785 g of Disodium Hydrogen Phosphate Dihydrate and 1.41 g of Sodium Dihydrogen Phosphate Dihydrate. In the 6.6 mmol phosphate buffer the formulation included 0.0357 g of Disodium Hydrogen Phosphate Dihydrate and 0.282 g of Sodium Dihydrogen Phosphate Dihydrate. In the 3.3 mmol phosphate buffer the formulation included 0.0182 g of Disodium Hydrogen Phosphate Dihydrate and 0.141 g of Sodium Dihydrogen Phosphate Dihydrate.

The formulation of the citrate buffer used in each sample included 600 g Purified Water, 1.141 g of Sodium Methyl Hydroxybenzoate *1 (equivalent of 0.96 g/L free acid), 0.563 g of Sodium Ethyl Hydroxybenzoate *1 (equivalent to 0.48 g/L free acid), 0.50 g Sucralose, 2.0 g of Raspberry Flavour, 2.520 g of Methotrexate Disodium (QS to 2.194 g/L) and made up to 1000 ml using Purified Water.

In the 100 mmol citrate buffer the formulation included 25.7 g of Sodium Citrate and 2.65 g of Citric Acid Monohydrate. In the 4.3 mmol citrate buffer the formulation included 1.18 g of Sodium Citrate and 0.1155 g of Citric Acid Monohydrate.

TABLE 5 Buffer Strength 5° C. 25° c. Phosphate 66 mmol PPT @ 2 M PPT @ 2 M Phosphate 33 mmol PPT @ 2 M CS @ 3 M Phosphate 6.6 mmol CS @ 3 M CS @ 3 M Phosphate 3.3 mmol CS @ 3 M CS @ 3 M Citrate 87 mmol PPT @ 1 week PPT @ 1 M Citrate 8.7 mmol PPT @ 3 M CS @ 4 M PPT—precipitate observed CS—Clear Solution. No precipitate 2 M represents 2 month time period 3 M represents 3 month time period 6 M represents 4 month time period

The results in table 5 support the results in table 4 in that the lower the ionic strength of the buffer system used in the formulation at pH 6.0, the more stable the Methotrexate formulation was over time.

Example 2 below shows a further Methotrexate formulation according to an embodiment of the present invention.

Example 2

Specifi- Ingredient cation Weight/5 ml Weight/liter Purified Water (A) Ph.Eur 3 ml 600.00 g Sodium Methyl Ph.Eur QS to 4.80 mg QS to 0.96 g Hydroxybenzoate Free acid free acid Sodium Ethyl Ph.Eur QS to 2.40 mg QS to 0.48 g Hydroxybenzoate free acid free acid Disodium Hydrogen Ph.Eur 5.72 mg 1.144 g Phosphate Dihydrate Citric Acid Monohydrate Ph.Eur 6.27 mg 1.254 g Raspberry Flavour 545742E HSE 10.0 mg 2.00 g Sucralose USP 2.5 mg 500.00 mg Purified water (B) Ph.Eur 0.375 ml 75.00 g Methotrexate Disodium Ph.Eur QS to 10.97 mg QS to 2.194 g (equivalent to 10 mg/5 ml Methotrexate base) Disodium Hydrogen HSE QS to pH QS to pH Phosphate Dihydrate (as a 10% ^(w)/_(v) solution) Citric Acid Monohydrate HSE QS to pH QS to pH (as a 10% ^(w)/_(v) solution) Purified Water (C) Ph.Eur To 5 ml To 1000 ml (1010.0 g*)g *based on weight per ml of 1.010 g/ml) Ph.Eur—European Pharmacopoeia HSE—In House Standard USP—United States Pharmacopoeia QS—Quantum Satis (Methotrexate Disodium and the Sodium p-Hydroxybenzoate preservatives are hygroscopic, therefore will require QS calculations prior to dispensing and batch manufacture.)

An example method of manufacture is set out below for the formulation shown in example 2. This method is typically undertaken at room temperature and pressure and could be carried out using a propeller mixer or a high shear mixer for example.

Manufacturing Process

-   1. Add the aqueous carrier agent in the form of Purified Water (A)     to the main manufacturing vessel. -   2. Add the preservatives in the form of Sodium Methylhydroxybenzoate     and Sodium Ethyl Hydroxybenzoate to the main vessel and mix until     substantially dissolved using a suitable mixer. -   3. Add the buffer agent Disodium Hydrogen Phosphate Dihydrate to the     main vessel and mix until substantially dissolved using a suitable     mixer. -   4. Add the buffer agent Citric Acid Monohydrate to the main vessel     and mix until substantially dissolved using a suitable mixer. -   5. Add the flavouring agent in the form of Raspberry Flavour to the     main vessel and mix until substantially dispersed using a suitable     mixer. -   6. Add the sweetening agent in the form of Sucralose to the main     vessel and mix until substantially dissolved using a suitable mixer. -   7. Into a suitable clean separate stage vessel dispense aqueous     carrier agent in the form of purified water (B). -   8. Add the Methotrexate Disodium salt into the separate stage vessel     and mix until substantially dissolved either by hand or using a     suitable mixer. -   9. Add the separate stage Methotrexate solution (from stage 8) into     the main vessel and mix until substantially dispersed using a     suitable mixer. -   10. Check the pH. If it is outside the range of 6.25+/−0.15 adjust     the pH until it is within this range by using either 10% w/v     solution of Citric Acid Monohydrate to lower the pH or a 10% w/v     solution of Disodium Hydrogen Phosphate Dihydrate to increase the     pH. -   11. Add Purified Water (C) to make to final weight and mix until     substantially dispersed using a suitable mixer. -   12. The finished product is filled into amber glass bottles.

While the invention has been described with a certain degree of particularity, it is manifest that many changes may be made in the details of construction and the arrangement of components without departing from the spirit and scope of this disclosure. It is understood that the invention is not limited to the embodiments set forth herein for purposes of exemplification, but is limited only by the scope of the attached claims, including the full range of equivalency to which each element thereof is entitled. 

What is claimed is:
 1. A method of treating rheumatoid arthritis in a patient; the method comprising administering to the patient in need thereof a methotrexate composition for oral administration consisting of a pharmaceutically acceptable salt of methotrexate, purified water, one or more buffer agents to adjust the pH of the composition to 6 to 7, and at least one agent selected from the group consisting of preserving agents, flavoring compounds, and sweetening agents.
 2. The method of claim 1, wherein the patient has difficulty swallowing.
 3. The method of claim 2, wherein the patient is a child.
 4. The method of claim 2, wherein the patient is elderly.
 5. The method of claim 1, wherein the rheumatoid arthritis is polyarthritic forms of active juvenile idiopathic arthritis.
 6. The method of claim 1, wherein the one or more buffer agents comprise any or any combination of citric acid, citric acid monohydrate, sodium citrate, sodium dihydrogen phosphate, disodium hydrogen phosphate, trometamol (Tris), hydrochloric acid, ascorbic acid, sodium ascorbate, any of the abovementioned sodium salts replaced with potassium salts.
 7. The method of claim 1, wherein the composition comprises two or more buffer agents to form a buffer system.
 8. The method of claim 1, wherein the buffer agents have a strength between 2 to 200 millimolar.
 9. The method of claim 1, wherein the buffer agents have a strength between 2 to 20 millimolar.
 10. The method of claim 1, wherein the preserving agents comprise any or any combination of sodium methyl hydroxybenzoate, sodium ethyl hydroxybenzoate, sodium propyl hydroxybenzoate, sodium benzoate, or potassium sorbate.
 11. The method of claim 1, wherein the one or more flavoring compounds and/or sweetening agents comprises sucralose, acesulfame K, any other water soluble sweetener, or raspberry flavor 545742E.
 12. The method of claim 1, wherein a pharmaceutically acceptable dosage of the methotrexate salt used is in the range of 0.05 mg/1 ml to 20 mg/1 ml.
 13. A method of treating leukemia in a patient; the method comprising administering to the patient in need thereof a methotrexate composition for oral administration consisting of a pharmaceutically acceptable salt of methotrexate, purified water, one or more buffer agents to adjust the pH of the composition to 6 to 7, and at least one agent selected from the group consisting of preserving agents, flavoring compounds, and sweetening agents.
 14. The method of claim 13, wherein the patient has difficulty swallowing.
 15. The method of claim 14, wherein the patient is a child.
 16. The method of claim 14, wherein the patient is elderly.
 17. The method of claim 13, wherein the leukemia is acute.
 18. The method of claim 13, wherein the one or more buffer agents comprise any or any combination of citric acid, citric acid monohydrate, sodium citrate, sodium dihydrogen phosphate, disodium hydrogen phosphate, trometamol (Tris), hydrochloric acid, ascorbic acid, sodium ascorbate, any of the abovementioned sodium salts replaced with potassium salts.
 19. The method of claim 13, wherein the composition comprises two or more buffer agents to form a buffer system.
 20. The method of claim 13, wherein the buffer agents have a strength between 2 to 200 millimolar.
 21. The method of claim 13, wherein the buffer agents have a strength between 2 to 20 millimolar.
 22. The method of claim 13, wherein the preserving agents comprise any or any combination of sodium methyl hydroxybenzoate, sodium ethyl hydroxybenzoate, sodium propyl hydroxybenzoate, sodium benzoate, or potassium sorbate.
 23. The method of claim 13, wherein the one or more flavoring compounds and/or sweetening agents comprises sucralose, acesulfame K, any other water soluble sweetener, or raspberry flavor 545742E.
 24. The method of claim 13, wherein a pharmaceutically acceptable dosage of the methotrexate salt used is in the range of 0.05 mg/1 ml to 20 mg/1 ml. 